SAETTINI, FRANCESCO
 Distribuzione geografica
Continente #
NA - Nord America 3.533
AS - Asia 2.307
EU - Europa 1.689
SA - Sud America 330
AF - Africa 54
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 7.917
Nazione #
US - Stati Uniti d'America 3.301
SG - Singapore 748
IT - Italia 594
VN - Vietnam 496
CN - Cina 370
HK - Hong Kong 318
RU - Federazione Russa 255
BR - Brasile 242
CA - Canada 177
DE - Germania 160
SE - Svezia 142
IE - Irlanda 128
GB - Regno Unito 110
IN - India 79
FR - Francia 71
BD - Bangladesh 58
FI - Finlandia 52
TR - Turchia 34
AR - Argentina 33
UA - Ucraina 30
NL - Olanda 29
PL - Polonia 28
ID - Indonesia 25
JP - Giappone 24
KR - Corea 23
MX - Messico 23
ES - Italia 22
IQ - Iraq 21
PH - Filippine 18
PK - Pakistan 18
ZA - Sudafrica 17
DK - Danimarca 16
AT - Austria 15
CO - Colombia 15
SA - Arabia Saudita 11
VE - Venezuela 11
AE - Emirati Arabi Uniti 10
IL - Israele 10
CR - Costa Rica 9
EC - Ecuador 7
EG - Egitto 7
HN - Honduras 7
MY - Malesia 7
TN - Tunisia 7
CH - Svizzera 6
KE - Kenya 6
LT - Lituania 6
MA - Marocco 6
UZ - Uzbekistan 6
CL - Cile 5
PE - Perù 5
UY - Uruguay 5
AZ - Azerbaigian 4
BZ - Belize 4
ET - Etiopia 4
JO - Giordania 4
KZ - Kazakistan 4
PT - Portogallo 4
PY - Paraguay 4
BH - Bahrain 3
NI - Nicaragua 3
NP - Nepal 3
PA - Panama 3
PS - Palestinian Territory 3
SI - Slovenia 3
AL - Albania 2
BE - Belgio 2
BG - Bulgaria 2
BO - Bolivia 2
CZ - Repubblica Ceca 2
DO - Repubblica Dominicana 2
GR - Grecia 2
JM - Giamaica 2
LB - Libano 2
NZ - Nuova Zelanda 2
RO - Romania 2
TW - Taiwan 2
AM - Armenia 1
AO - Angola 1
AU - Australia 1
BW - Botswana 1
BY - Bielorussia 1
CY - Cipro 1
DZ - Algeria 1
EE - Estonia 1
GA - Gabon 1
GE - Georgia 1
GH - Ghana 1
GT - Guatemala 1
GY - Guiana 1
HU - Ungheria 1
KG - Kirghizistan 1
KW - Kuwait 1
LV - Lettonia 1
LY - Libia 1
MT - Malta 1
NG - Nigeria 1
NO - Norvegia 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
Totale 7.916
Città #
Ann Arbor 597
Singapore 448
Ashburn 364
Hong Kong 307
San Jose 262
Milan 191
Chandler 161
Ho Chi Minh City 158
Fairfield 154
Dublin 127
Hanoi 127
Toronto 125
Wilmington 111
Los Angeles 103
New York 102
Frankfurt am Main 101
Houston 83
Dallas 76
Santa Clara 65
Beijing 64
Seattle 53
The Dalles 52
Hefei 51
Woodbridge 51
Chicago 48
Buffalo 42
Princeton 38
Cambridge 37
Helsinki 34
São Paulo 32
Shanghai 31
Lauterbourg 29
Rome 28
Moscow 27
Da Nang 25
Boardman 23
Munich 23
Seoul 22
Dearborn 21
Montreal 21
Warsaw 21
Tokyo 20
Altamura 19
Council Bluffs 19
London 19
Chennai 18
Lawrence 18
Manchester 18
Monza 18
Denver 17
Orem 17
Jacksonville 16
Jakarta 16
Phoenix 16
Brooklyn 15
Boston 14
Haiphong 14
Atlanta 13
San Diego 12
Nanjing 11
Turku 11
Biên Hòa 10
Can Tho 10
Ha Long 10
Hải Dương 10
Stockholm 10
Turin 10
Washington 10
Casalecchio di Reno 9
Como 9
Johannesburg 9
Baghdad 8
City of London 8
Florence 8
Guangzhou 8
Ottawa 8
Seregno 8
Vienna 8
Ankara 7
Bologna 7
Changsha 7
Figino 7
Lissone 7
Medellín 7
Nuremberg 7
Poplar 7
Pune 7
Quận Một 7
Rio de Janeiro 7
San Francisco 7
San José 7
Belo Horizonte 6
Columbus 6
Curitiba 6
Guarulhos 6
Istanbul 6
Karachi 6
Kuala Lumpur 6
Paris 6
Tashkent 6
Totale 5.054
Nome #
Cardiofaciocutaneous syndrome and immunodeficiency: data from an international multicenter cohort 447
Biallelic PI4KA Mutations Disrupt B-Cell Metabolism and Cause B-Cell Lymphopenia and Hypogammaglobulinemia 407
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency 386
A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency 370
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients 348
Two siblings presenting with novel ADA2 variants, lymphoproliferation, persistence of large granular lymphocytes, and T-cell perturbations 329
Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome 315
Pediatric immune myelofibrosis (PedIMF) as a novel and distinct clinical pathological entity 310
Primary immunodeficiencies, autoimmune hyperthyroidism, coeliac disease and systemic lupus erythematosus in childhood immune thrombocytopenia 297
A novel homozygous disruptive PRF1 variant (K285Sfs*4) causes very early-onset of familial hemophagocytic lymphohystiocytosis type 2 295
Early diagnosis of PI3Kδ syndrome in a 2 years old girl with recurrent otitis and enlarged spleen 286
Antibody Deficiency in Patients with Biallelic KARS1 Mutations 284
Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome 282
Secondary hemophagocytic lymphohystiocytosis in a Rubinstein Taybi syndrome patient 265
Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis 256
Ruptured hepatoblastoma: A case report and literature review 255
When to suspect GATA2 deficiency in pediatric patients: from complete blood count to diagnosis 251
More than an ‘atypical’ phenotype: dual molecular diagnosis of autoimmune lymphoproliferative syndrome and Becker muscular dystrophy 246
Neutropenia, hypogammaglobulinemia, and pneumonia: A case of WHIM syndrome 228
Hermansky-Pudlak syndrome type II and lethal hemophagocytic lymphohistiocytosis: Case description and review of the literature 228
Isolated leukopenia in children and adolescents referred to a Pediatric Hematology Clinic 225
Correction to: Antibody Deficiency in Patients with Biallelic KARS1 Mutations (Journal of Clinical Immunology, (2023), 43, 8, (2115-2125), 10.1007/s10875-023-01584-7) 220
Is multifocality a prognostic factor in childhood hepatoblastoma? 219
Finding balance between mature and immature neutrophils: The effects of empagliflozin in GSD-Ib 208
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype 200
Bone Marrow CD8 + Abundance Inversely Correlates with Progressive Marrow Fibrosis and Myelodysplastic Evolution in GATA2 Deficiency: Case Report 198
Severe and recurrent infections identify severe congenital neutropenia and primary immunodeficiencies in pediatric isolated neutropenia 169
A novel germline mutation of ada2 gene in two “discordant” homozygous female twins affected by adenosine deaminase 2 deficiency: Description of the bone-related phenotype 168
SYNDROMES, GENETICS AND IMMUNOLOGY: FROM THE BEGINNING OF THE END TO THE END OF THE BEGINNING [Sindromi, genetica e immunologia: dall'inizio della fine alla fine dell'inizio] 165
Clinical features of Epstein-Barr virus infection in primary immunodeficiency patients 148
The novel XIAP Lys396Ter variant alters mitochondrial membrane potential and endoplasmic reticulum intensity in monocytes of two XIAP-deficient patients 130
Successful Treatment of Multirefractory Immune Thrombocytopenia in Rubinstein–Taybi Syndrome With Combined Rituximab and Eltrombopag 39
Totale 8.174
Categoria #
all - tutte 25.193
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 25.193


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022471 52 56 53 39 37 38 13 32 27 38 30 56
2022/2023588 56 188 26 65 32 77 9 46 51 5 16 17
2023/2024500 17 15 37 40 61 132 98 15 24 17 6 38
2024/20251.379 46 109 78 75 159 66 102 68 139 216 117 204
2025/20263.922 611 310 273 495 439 191 557 123 204 316 201 202
2026/202748 48 0 0 0 0 0 0 0 0 0 0 0
Totale 8.174